- Polymerase Chain Reaction and Heteroduplex Analysis Based Detection of Clonal T Cell Receptor Gamma Gene Rearrangements in Paraffin-embedded Tissues of Cutaneous T Cell Proliferative Diseases
-
Yeo UC, Park K, Ko YH, Lee ES, Han KH, Kim CW, Cho KH
- KMID: 2163882
- Ann Dermatol.
- 2001 Sep;13(3):139-147.
- doi: 10.5021/ad.2001.13.3.139
BACKGROUND: Recently, the molecular pathologic investigation for clonality in lymphomas has been introduced and has gained a role in the diagnosis of lymphomas. In fact, the clonality test using TCRGR... -
- CITED
-
- Close
- SHARE
-
- Close
- Molecular Diagnosis of Cutaneous T Cell Lymphoproliferative Diseases
-
Park JY, Lee MH, Kwak EK, Kim DJ, Park TI, Bae HI
- KMID: 1725736
- Korean J Pathol.
- 2000 Nov;34(11):941-949.
It is often problematic to diagnose T-cell lymphoproliferative disorders of the skin because of the difficulty in establishing clonality in paraffin-embedded tissue. We used polymerase chain reaction single strand conformational... -
- CITED
-
- Close
- SHARE
-
- Close
- Diagnostic Utility of Polymerase Chain Reaction-Based Clonality Analysis for Immunoglobulin Heavy Chain Gene and T-cell Receptor Gamma Chain Gene Rearrangement in Lymphoid Neoplasms
-
Cho EY, Ko YH, Kim DS, Han JJ, Ree HJ
- KMID: 2275585
- Korean J Pathol.
- 2001 Dec;35(6):461-469.
BACKGROUND: The clonality of lymphoid infiltrates determined by polymerase chain reaction (PCR) for immunoglobulin heavy chain (IgH) or T cell receptor (TCR) genes is not only useful in confirming the... -
- CITED
-
- Close
- SHARE
-
- Close
- Molecular Diagnosis of 21-hydroxylase (CYP21) Gene mutations in Congenital Adrenal Hyperplasia
-
Lee HS, Cheon KW, Park YS, Han IK, Kang IS
- KMID: 2262293
- Korean J Obstet Gynecol.
- 2001 Jun;44(6):1171-1177.
OBJECTIVES: Congenital adrenal hyperplasia (CAH) is an autosomal recessive disease which is most often caused by a deficiency in steroid 21-hydroxylase (21-OH), a microsomal enzyme encoded by the CYP21 gene.... -
- CITED
-
- Close
- SHARE
-
- Close
- Familial Writer's Cramp with DYT1 Mutation: A Clinical and Genetic Analysis of a New Kindred
-
Lee JK, Im JH, Lee MC
- KMID: 2186025
- J Korean Neurol Assoc.
- 2001 Mar;19(2):110-115.
BACKGROUND: Recently a non-Jewish German family with writer's cramp was reported to have DYT1 mutation, expanding the phenotypic spectrum of DYT1. Although functional brain surgery has been tried for generalized... -
- CITED
-
- Close
- SHARE
-
- Close
- Characterization of clonal immunoglobulin heavy (IGH) V-D-J gene rearrangements and the complementarity-determining region in South Indian patients with precursor B-cell acute lymphoblastic leukemia
-
Sudhakar N, Rajkumar T, Rajalekshmy KR, Nancy NK
- KMID: 2375205
- Blood Res.
- 2017 Mar;52(1):55-61.
- doi: 10.5045/br.2017.52.1.55
BACKGROUND: This study characterized clonal IG heavy V-D-J (IGH) gene rearrangements in South Indian patients with precursor B-cell acute lymphoblastic leukemia (precursor B-ALL) and identified age-related predominance in VDJ rearrangements. METHODS:... -
- CITED
-
- Close
- SHARE
-
- Close
